Myungmoon Amoxylan Duo Syrup [Amoxicillin Trihydrate · Clavulanate Potassium (7:1)]

Adult dose

For recurrent tonsillitis and other upper respiratory infections, lower respiratory infections, urinary tract infections, and mild to moderate skin and soft tissue infections, administer 25 mg of amoxicillin/3.6 mg of clavulanate per kg of body weight divided into 2 doses daily. For moderate to severe infections such as otitis media and sinusitis, and lower respiratory infections such as bronchopneumonia, administer 45 mg of amoxicillin/6.4 mg of clavulanate per kg of body weight divided into 2 doses daily. Potential

Child dose

The 7:1 syrup is not suitable for children under 2 months. It is not appropriate for pediatric patients with renal insufficiency.

This medication should not be used in patients with hypersensitivity to specific components or to beta-lactam antibiotics. Additionally, it should be avoided in patients with viral infections such as infectious mononucleosis or lymphocytic leukemia, as the risk of rash is increased. Patients who have previously experienced jaundice or liver dysfunction due to this medication or penicillin-related drugs should be cautious as symptoms may recur upon use. It contains lactose, so it should not be given to patients with lactose intolerance or galactose metabolism disorders. Patients with impaired liver function should use this medication with caution, and those with moderate or severe renal impairment may require adjustments to the dosing interval due to the potential for increased drug concentrations. Patients with a history of allergies or frequent allergic symptoms such as asthma, rashes, or hives should also be carefully monitored during treatment. Patients with severe gastrointestinal disorders, such as vomiting or diarrhea, should be cautious as the drug may not be adequately absorbed. This medication may cause gastrointestinal side effects such as diarrhea, vomiting, and abdominal pain; if severe diarrhea or abdominal pain persists, discontinue use immediately and consult a doctor. Liver function abnormalities may also occur rarely, and this is reported more frequently in older adults or males, so regular liver function testing is advisable. Severe allergic reactions such as hives, significant swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions, high fever with severe rashes, blisters, skin peeling, mucosal pain in the mouth or eyes, severe skin reactions, difficulty breathing or dyspnea, asthma attacks, respiratory issues accompanying cough and fever, jaundice, generalized fatigue, liver abnormalities, sudden and severe symptoms can occur; discontinue use immediately if these occur. Blood abnormalities have been reported infrequently, such as leukopenia, anemia, and thrombocytopenia, which may require regular blood testing. Central nervous system symptoms such as anxiety, confusion, and seizures may rarely occur; notify a doctor if neurological symptoms arise. Patients with compromised kidney function are at risk for acute kidney failure, thus renal function should be monitored regularly. This medication can affect the balance of intestinal bacteria, leading to fungal infections such as candidiasis; consult a doctor if symptoms occur. Long-term use may lead to a tendency to bleed due to vitamin K deficiency, so caution is needed. There may be interactions with other medications while using this drug, so inform your healthcare provider of any other medications being taken. Avoid use in the first three months of pregnancy, and exercise caution during pregnancy only when the benefits outweigh the risks. During breastfeeding, this medication may pass into breast milk and cause side effects in the infant; discontinue use if side effects are observed. It is not recommended for premature infants or newborns (under 2 months) as safety has not been established. Elderly patients are at higher risk of side effects due to declining bodily functions, thus monitoring dosage and administration intervals closely is advised. This medication may affect blood and urine test results, so inform medical personnel at the time of testing. In case of overdose, gastrointestinal symptoms, rash, drowsiness, and seizures may occur; discontinue use immediately and seek appropriate treatment. After preparation, this medication should be stored in a sealed container away from air and moisture, and kept in a cool, dry place at a temperature below 25 degrees Celsius to maintain effectiveness.

Serious side effects

Hives, severe swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions, high fever with severe rash, blisters, skin peeling, pain in mucous membranes of mouth/eyes, severe skin abnormal reactions, shortness of breath or difficulty in breathing, asthma attacks, breathing issues associated with cough and fever, jaundice, generalized extreme fatigue, liver abnormalities, abrupt and very severe symptoms

Mild side effects

• Diarrhea
• pseudomembranous colitis
• dyspepsia
• stomatitis
• gastritis
• glossitis
• nausea
• vomiting
• loss of appetite
• abdominal pain

This medication should be stored in a tightly sealed container to prevent exposure to air and moisture and should be kept in a cool and dry place below 25 degrees Celsius.

Appearance

A white or pale yellow powder that is used as a syrup after being dissolved.

Package unit

50mL(5.5057g) × 1 bottle